| Titre : | Association Between the Ubiquitin Carboxyl-Terminal Esterase L1 Gene (UCHL1) S18Y Variant and Parkinson's Disease : A HuGE Review and Meta-Analysis. (2009) |
| Auteurs : | Margaret RAGLAND ; Karen EDWARDS ; Carolyn HUTTER ; ZABETIAN (Cyrus) : USA. Geriatric Research Education and Clinical Center. Veterans Affairs Puget Sound Health Care System. Seattle. WA. ; Department of Epidemiology. University of Washington School of Public Health. Seattle. WA. USA ; Institute for Public Health Genetics. University of Washington School of Public Health. Seattle. WA. USA |
| Type de document : | Article |
| Dans : | American journal of epidemiology (vol. 170, n° 11, 2009) |
| Pagination : | 1344-1357 |
| Langues: | Anglais |
| Mots-clés : | Association ; Gène ; Génétique ; Homme ; Enquête cas témoin ; Epidémiologie ; Enzyme ; Maladie dégénérative |
| Résumé : | [BDSP. Notice produite par INIST-CNRS R0xHoBp9. Diffusion soumise à autorisation]. The ubiquitin carboxyl-terminal esterase L1 gene, UCHL1, located on chromosome 4p14, has been studied as a potential candidate gene for Parkinson's disease risk. The authors conducted a Human Genome Epidemiology review and meta-analysis of published case-control studies of the UCHL1 S18Y variant and Parkinson's disease in Asian and Caucasian samples. The meta-analysis of studies in populations of Asian ancestry showed a statistically significant association between the Yallele and reduced risk of Parkinson's disease under a recessive model (odds ratio (OR) for YY vs. SY+SS=0.79,95% confidence interval (CI) : 0.67,0.94 ; P=0.006). For a dominant model, the association was not significant in Asian populations (OR for YY+SY vs. SS=0.88,95% CI : 0.68,1.14 ; P=0.33). For populations of European ancestry, the meta-analysis showed a significant association between the Y allele and decreased risk of Parkinson's disease under a dominant model (OR=0.89,95% CI : 0.81,0.98 ; P=0.02) but not under a recessive model (OR=0.92,95% CI : 0.66,1.30 ; P=0.65). Using the Venice criteria, developed by the Human Genome Epidemiology Network Working Group on the assessment of cumulative evidence, the authors concluded that moderate evidence exists for an association between the S18Y variant and Parkinson's disease. |
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